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FAM13B

family with sequence similarity 13 member B

HCNC Approved Symbol
FAM13B (HGNC:1335)
Genomic Coordinates
5:137,937,960 - 138,052,178 (5q31.2)
Synonyms
N61, KHCHP, ARHGAP49, C5orf5, FAM13B1
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there is 1 patient* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

FAM13B - Gene browser | 3billion